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. 2015 Aug 26;6:424. doi: 10.3389/fimmu.2015.00424

Table 1.

Therapeutic efficacy and related toxicities of drugs developed for cancer treatment.

Therapeutic strategy Target Clinical benefit Toxicity Reference
IMMUNOTHERAPY
Ipilimumab Anti-CTLA-4 Increased OS from 6.4 to 10 months 15% had grade 3 or 4 AE (55)
Pembrolizumab Anti-PD-1 Response rate of 38% Grade 1 or 2 AE (56)
Ipilimumab + Nivolumab Anti-CTLA-4 plus Anti-PD-1 Objective response 53% 50% had grade 3 or 4 AE (57)
BMS-93655 Anti-PD-L1 Objective response 6%–17% 9% had grade 3 or 4 AE (58)
MONOCLONAL ANTIBODIES
Trastuzumab Anti-HER2/neu Increased OS from 20.3 to 25.1 months 27% had cardiac toxicity (59)
Bevacizumab Anti-VEGF Increased OS from 15.6 to 20.3 months Grade 3 hypertension (60)
Rituximab Anti-CD20 Clinical remission in 46% of patients Grade 1 or 2 AE (61)
VACCINES
Provenge PAP plus GM-CSF Increased OS from 21.7 to 25.8 months Grade 1 or 2 AE (62)
Gardasil HPV type 6, 11, 16, and 18 Efficacy was 98% Grade 1 or 2 AE (63)
Pemetrexed MAGE-A3 + TLR4 + TLR9 No difference in OS 9% had grade 3 or 4 AE (64)
Synthetic long-peptide HPV-16 E6 plus HPV-16 E7 Response rate of 79% Grade 1 or 2 AE (65)
ADOPTIVE CELL TRANSFER
T-cells MART-1 or gp100 Response rate of 46% Autoimmune events (66)
Naïve T-cells LY6K-177 peptides Response rate of 22% Grade 1 or 2 AE (67)
Memory T-cells MCF-7 cell lysate antigen Increased OS to 33.8 months No toxicity noted (68)
CAR therapy Modified CD19 Response rate of 90% Cytokine release syndrome (69)
CAR therapy GD2 antigen Median OS 931 days 15% had grade 1 or 3 AE (70)

AE, adverse event; HPV, human papillomavirus; OS, overall survival; PAP, prostatic acid phosphatase.